Distal myopathy, Nonaka type Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms. (Human Disease Ontology, DOID_3429)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536816
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Genes

1 genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase 2.88009